Canonical Allele Identifier: CA1696187026

Gene: HOXA1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095581T= , CM000669.2:g.27095581T=	GRCh38
NC_000007.13:g.27135200T= , CM000669.1:g.27135200T=	GRCh37
NC_000007.12:g.27101725T=	NCBI36
NG_011813.1:g.5426A=
NG_033087.1:g.4488T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.332A= MANE Select	ENSP00000494260.2:p.Tyr111=
ENST00000343060.4:c.332A=	ENSP00000343246.4:p.Tyr111=
ENST00000355633.5:c.332A=	ENSP00000347851.5:p.Tyr111=
NM_005522.4:c.332A=	NP_005513.1:p.Tyr111=
NM_153620.2:c.332A=	NP_705873.2:p.Tyr111=
NM_005522.5:c.332A= MANE Select	NP_005513.2:p.Tyr111=
NM_153620.3:c.332A=	NP_705873.3:p.Tyr111=